Job Title: Environmental Monitoring Technicians- I The Merck Manufacturing Operations teams are the people that make our products. The Laboratory Technician position at the Elkton, Virginia Manufacturing site is a key contributor in our Quality Operations units that helps ensure products made are safe and compliant. Location: Elkton, VA 22827$63k-82k yearly est.3d ago
Remote- Statistical Project Leader
As a Statistical Project Leader, you will provide statistical leadership and guidance for clinical studies in one or more indications and will be accountable for methodological and statistical aspects of clinical development or medical affairs plans and subsequent deliverables. #LI-SA At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values.$180.7k yearly8d ago
Senior Technician-Utilities-HVAC-2nd Shift
We have a strong portfolio of leading consumer healthcare products (Bayer Aspirin, Aleve, Claritin, One A Day, Flintstones Vitamins, Phillips' and more) Then Bayer is the place for you.$97k-124k yearly est.5d ago
Market Access Manager Industry Partners Poultry (m/f/d)
Wir suchen ab sofort eine/n Market Access Manager Industry Partners Poultry (m/w/d) f r die strukturierte Betreuung und Kommunikation von und mit Key Stakeholdern im landwirtschaftlichen Umfeld der Gefl gelindustrie DACH-Region.$111k-148k yearly est.4d ago
Sales Rep. Vision EDOMEX (Privado y Gobierno)
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.
Representante de ventas Lilly: El Orquestador del negocio
En Eli Lilly buscamos personas apasionadas que se unan a nuestro propósito de mejorar la vida de las personas en el mundo.Vivimos en un mundo de constante cambio y evolución y en Lilly, somos conscientes del impacto que esto tiene en nuestro negocio y forma de trabajo, lo cual nos impulsa a tomar lo que tenemos y hacerlo mejor y mejor cada día.La fuerza de ventas de Lilly necesita más que representes de ventas… orquestadores de ventas , que se adueñen del negocio y tomen los recursos disponibles para maximizarlos de forma estratégica e impactar de forma positiva a nuestros principales clientes con el propósito de mejorar la vida de las personas en el mundo. Cómo es el día a día de esta posición?Entender, implementar y comunicar efectivamente la estrategia comercial mediante la promoción de nuestros productos.Aplicar los recursos multicanal (digital y presencial) disponibles, de forma adecuada y estratégica en el canal correcto con el cliente correcto.Analizar tu negocio para tomar decisiones que te permitan hacerlo crecer.Visitar a los médicos y farmacias en el tiempo correcto y con la frecuencia correcta.Accionar siempre con los más altos estándares de ética y responsabilidad. Qué habilidades buscamos?:Incluir: Trabajar en equipo creando un ambiente diverso e inclusivo, comunicándose de forma efectiva con colaboradores y clientes e influenciar de forma positiva con o sin autoridad.Innovar: Pensar y ser curioso en búsqueda de la mejora continua, adaptarse al cambio constante, ser creativo e invertir tiempo en su propio desarrollo.Acelerar: Pensar estratégicamente y analizar para tomar decisiones ágiles, resolver problemas de forma rápida y efectiva, planear y organizarse ante un ambiente diverso y con constantes accionables, sobreponer obstáculos y trabajar con inteligencia emocional.Cumplir: Mostrar disciplina en ejecución con respecto a la visita médica, maximización de recursos multicanal y demostrar coraje e integridad día a día. Esta posición es para ti si:Estas titulado de cualquier licenciatura o ingeniería.Nivel inglés intermedio-alto.Experiencia conduciendo y contar con licencia de manejo vigente.Manejo de plataformas tecnológicas relacionadas con análisis de información y comunicación virtual.Manejo mercado de GobiernoLo que nosotros ofrecemos Salario competitivo y un amplio portafolio de beneficios extralegales.Un ambiente de trabajo construido sobre el trabajo en equipo, flexibilidad y respeto.Crecimiento profesional, y programas de desarrollo para ejecutar un plan de carrera dentro de la compañía.Programas de bienestar laboral y medicina integral para tí y tu familia.Flexibilidad laboral.Zona de trabajo: Atizapán y TlalnepantlaViaje: No aplica Modalidad: Remoto (Los representantes de ventas laboran dentro de un territorio asignado) Horarios de acuerdo a los clientes (Médicos).
Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( Lilly_Recruiting_Compliance@lists.lilly.com ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response.
Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
#WeAreLilly$77k-116k yearly est.Easy Apply4d ago
Senior / Executive Director - Global Medical Affairs, Diabetes and Obesity Business Unit
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.
Purpose:
Through the application of scientific and medical training, clinical expertise, and relevant clinical experience, the Diabetes and Obesity Business Unit - Global Medical Affairs Senior/Executive Director is an integral member of the medical affairs team for strategic planning in the support of launch and commercialization activities to meet patients' needs and ultimately enhance the customers' experience in interacting with the company. The definition of “customer” here includes patients, providers (HCPs) and payers. The Senior/Executive Director may also work closely with global Development teams, Therapeutic Area Program Phase, Early Phase / Clinical Pharmacology, and Translational Medicine teams in new product development activities over the entire spectrum of drug development and clinical trial phases. Specific activities include developing or contributing to the global and/or regional clinical/medical plan in his/her therapeutic area of responsibility, the development, conduct and reporting of clinical trials; the implementation of global clinical trials conducted in local affiliates/countries; the reporting of adverse events as mandated by corporate patient safety; review process for protocols, study reports, publications and data dissemination for products; new and updated labels, documents and tools supporting product pricing, reimbursement, and access (PRA), grant submissions and contracts; contacts with regulatory and other governmental agencies; the outreach medical activities aimed at the external clinical customer community, including thought leaders; and various medical activities in support of demand realization
The Senior/Executive Director serves as a scientific resource for study teams, departments, and others as needed. The Senior/Executive Director is aware of and ensures that all activities of the medical team (and direct reports, if applicable) are in compliance with current local and international regulations, laws, guidance (for example, FDA, ICH, and CPMP etc.), Good Clinical Practices (GCPs), company standards, Lilly policies and procedures, global quality standards, the Principles of Medical Research and activities are aligned with the medical vision.
Primary Responsibilities:
The primary responsibility of the Diabetes and Obesity Business Unit - Medical Affairs Senior/Executive Director is to provide expert medical support to all aspects of the local/global business, to ultimately enhance the customers' experience in interacting with the company. This includes marketed product support (participate in the development of the “patient journey” and the strategic plan for the compound), medical support for regulatory affairs and interactions with government agencies (medical support for New and Supplemental New Drug Submissions and participating and presenting at meetings with government regulatory agencies), medical support for pricing, reimbursement and access(PRA) (providing medical guidance on the PRA plan and interacting with government PRA agencies as needed), and leading in scientific data dissemination (leading and presenting at conferences, advisory boards, etc., and overseeing the development of the scientific content of educational programs). These responsibilities are generally related to late-phase and marketed compounds, but can also include early phase trials (for example, phase I and II trials). The Senior/Executive Director is responsible for the planning, startup and conduct of phase 3b/4 studies , as well as non clinical trial solutions/activities that are conducted in the global team in affiliates/countries as described in the clinical plan. With the expansion of the Lilly portfolio, this role will be responsible for leadership that allows appropriate scientific support for incretins family within the portfolio and across the spectrum of patients with obesity. This includes, but is not limited to, design and execution of phase 3b/4 studies and expansion of real-world evidence, observational data and patient reported outcomes to address the needs of the commercial organization.
Business/ customer support (pre and post launch support)
Support the planning of symposia, advisory board meetings, and and/or the facilitation of other meetings with health care professionals. Support medical information associates in preparation and review of medical letters and other medical information materials. Support training of medical personnel, including medical and/or outcome liaisons and health outcomes staff. Prepare or review scientific information in response to customer questions or media requests. Provide follow-up to information requested by health care professionals as per global SOPs.
Support data analysis and the development of slide sets (through reviewing and/or approving) and publications (abstracts, posters, manuscripts). Establish and maintain appropriate collaborations and relationships with external scientific experts, thought leaders, and the general medical community on a local, national, regional, and possibly international basis. Develop and maintain appropriate collaborations and relationships with relevant professional societies. Support the design of customer research as medical expert. Provide congress support (for example, availability to answer questions at exhibits, provide oral and poster presentations, staff medical booth, meet thought leaders, and participate in customer events).
Participate in data analyses, development of scientific data dissemination, and preparation of final reports and publications. Participate in reporting of clinical trial data in Clinical Trial Registry activities.
Clinical Planning
Collaborate with Clinical Research Scientists (CRSs), regional clinical operations staff, statisticians, health outcomes, research scientists and selected investigators in the development of protocols and data collection requirements. Participate in investigator identification and selection, in conjunction with clinical teams. Ensure that the clinical operations team has documented the completion of administrative requirements for study initiation and conduct (i.e., ethical review board, informed consent, regulatory approval/notification) consistent with Good Clinical Practices (GCPs) and local laws and requirements. Assist in the planning process and participate in study start-up meetings and other activities to provide the appropriate scientific training and information to investigators and site personnel. Serve as resource to clinical research site monitors, investigators and ethical review boards to address any questions or clarify issues arising during the conduct of study.
Review IIT proposals and publications, as requested Contribute to global alignment of Phase 3b/4 clinical studies (and Phase I and II studies where applicable) planned by country (ies) or global Development team. Understand and actively address the scientific information needs of all investigators and personnel. Monitor patient safety during the conduct of studies and conduct the appropriate tracking and follow-up of adverse events, in alignment with corporate patient safety policies and procedures.
Regulatory Support Activities
Be aware of current trends and projections for clinical practice and access in the therapeutic area(s) relevant to the product, both near term (1-2 years) and longer-term (3-5 years). Critically read and evaluate the relevant medical literature; know the status and data from competitive products; and keep updated with medical and other scientific developments relevant to the product. Responsible for the scientific training of the clinical study team. Acts as scientific consultant and protocol expert for clinical study team members and others in medical. Explore and take advantage of opportunities for extramural scientific experiences.
Attend, contribute and participate in medical congresses/scientific symposia.
General Responsibilities
This Medical Affairs Sr/Executive Medical Director will primarily support launch activities outside the U.S.Be an ambassador of both patients and the Lilly Brand.
Minimum Qualification Requirements:
Medical Doctor or Doctor of Osteopathy. Must be board eligible or certified in appropriate specialty/subspecialty or have completed the comparable level of post-medical school clinical training relevant to the country of hiring. U.S. trained physicians must have achieved board eligibility or certification.Foreign medical graduates in U.S. based jobs, who are not U.S. board eligible or certified may be hired directly for employment in the U.S. at the discretion of the Chief Medical Officer. Non-U.S. trained physicians must have completed education and training at a medical school that meets the requirements of the Liaison Committee on Medical Education (LCME). For the recognized list of foreign medical schools and the disapproved list, see http://www.in.gov/pla/2799.htm
Preferences:
Board certified / Licensed Clinician in Endocrinology and Metabolism highly preferred Previous pharmaceutical experience in medical affairs and/or development highly preferred.Experience in Obesity disease state Knowledge of drug development process preferred Demonstrated ability to balance scientific priorities with business priorities Demonstrated strong individual leadership, communication, teamwork, organizational and negotiation skills Demonstrated ability to influence others (both cross-functionally and within the function) in order to create a positive working environment. Ability to engage in domestic and international travel to the degree appropriate to support the business of the team. Fluent in English, verbal and written communication.
Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( Lilly_Recruiting_Compliance@lists.lilly.com ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response.Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women's Network, Working and Living with Disabilities. Learn more about all of our groups.
#WeAreLilly$115k-180k yearly est.Easy Apply4d ago
Product Owner/ Business Analyst - Supply Chain Collaboration - US Remote
At Amgen, our shared mission-to serve patients-drives all that we do. Product Owner/ Business Analyst - Supply Chain Collaboration - US Remote$136.7k-161.3k yearly1d ago
Senior Associate Regulatory Affairs (Open to remote)
* Approve drug shipment for Amgen and Investigator Initiated Studies At Amgen, our shared mission-to serve patients-drives all that we do. Senior Associate Regulatory Affairs (Open to remote)$83.3k-104.4k yearly3d ago
Associate Vice President, Assistant General Counsel, Regulatory Legal Team, International
The Associate Vice President (AVP), Assistant General Counsel will be part of the Regulatory Legal Team (RLT), which reports up through Lilly's General Counsel and works across Lilly Legal and the Company with a highly cross-functional approach.$126k-163k yearly est.Easy Apply4d ago
Pricing Specialist
The Pricing Specialist is responsible for supporting the effectiveness and continued development of all pricing tools and systems including PROS, coordination of pricing, discounting, and account data to Distribution Pricing portal, and within SAP. We are seeking a Pricing Specialist to support the growth of our business.$59k-80k yearly est.4d ago
Senior Clinical Scientist - Cardiometabolic
We are known as Merck & Co., Inc., Rahway, New Jersey, USA in the United States and Canada and MSD everywhere else.$107.6k-169.4k yearly8d ago
Sr. Director - Counsel - Consumer / Customer Operations
$168k-246.2k yearlyEasy Apply4d ago
Senior Customer Support Associate
Exhibit conduct that is consistent with the Zoetis Mission and Vision, and with its Core Beliefs of:Our colleagues makes the difference;Run it like you own it;Customer obsessed;One ZoetisPerform duties in a safe manner. Enter and manage customer accounts and orders in Zoetis enterprise systems, including Salesforce and internal genetic databases.Manage customer communications via email. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume. Answer incoming phone calls and emails daily from customers, responding to their needs for product and or information; apply your knowledge of systems and required techniques to effectively satisfy customer orders and needs; provide answers to general inquiries regarding routine product use and services provided by Zoetis Genetics, sending additional information when necessary. Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property.$47k-68k yearly est.Easy Apply4d ago
Lead Clinical Data Manager (Early Development)
$103k-129k yearly est.4d ago
Remote- Statistical Project Leader
As a Statistical Project Leader, you will provide statistical leadership and guidance for clinical studies in one or more indications and will be accountable for methodological and statistical aspects of clinical development or medical affairs plans and subsequent deliverables. #LI-SA At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values.$180.7k yearly8d ago
Associate Clinical Research Associate - Southeast Region (REMOTE)
With support of Senior Clinical Research Associate (CRA)/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites.$72.9k-114.6k yearly2d ago
Senior Director- Consultant Relations
$138.8k-203.5k yearlyEasy Apply4d ago
Key Account Executive
Key Account Executive Costa Atl ntica$124k-162k yearly est.Easy Apply4d ago
Application Security Assessment Manager US Remote
Responsibilities: Lead both strategic and execution delivery responsibilities for application security related services Responsible for prioritization and managing resources in application vulnerability management both domestically and internationally to ensure initiatives are running effectively and in compliance with corporate standards Perform deep architecture and security reviews on complex enviornonments to identify vulnerabilities and assess the effectiveness of existing controls. This position is responsible for leading application security assessments throughout the organization This includes but is not limited to web applications, mobile applications, business applications and IoT devices Assessments include vulnerability identification, analysis, remediation guidance, and reporting.$99k-143k yearly4d ago
Safety Data Analyst, Senior Manager (US-Remote)
At Amgen, our shared mission-to serve patients-drives all that we do.$136.8k-152k yearly2d ago
